esv3646881

Organism: Homo sapiens

Study:estd214 (1000 Genomes Consortium Phase 3)
Variant Type:mobile element insertion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:43
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):1000 Genomes Project Consortium et al. 2015

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 251 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):32,361,536-32,361,536

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3646881	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
esv3646881	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000021.8	Chr21	33,733,845	33,733,845

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16313355	line1 insertion	SAMN00004625	Sequencing	Read depth and paired-end mapping	Heterozygous	2,591
essv16313356	line1 insertion	SAMN00004634	Sequencing	Read depth and paired-end mapping	Heterozygous	2,737
essv16313357	line1 insertion	SAMN00006340	Sequencing	Read depth and paired-end mapping	Heterozygous	2,731
essv16313358	line1 insertion	SAMN00004655	Sequencing	Read depth and paired-end mapping	Heterozygous	2,454
essv16313359	line1 insertion	SAMN00004668	Sequencing	Read depth and paired-end mapping	Heterozygous	2,231
essv16313360	line1 insertion	SAMN00016965	Sequencing	Read depth and paired-end mapping	Heterozygous	2,566
essv16313361	line1 insertion	SAMN00016979	Sequencing	Read depth and paired-end mapping	Heterozygous	2,879
essv16313362	line1 insertion	SAMN00006376	Sequencing	Read depth and paired-end mapping	Heterozygous	2,448
essv16313363	line1 insertion	SAMN00009108	Sequencing	Read depth and paired-end mapping	Heterozygous	2,494
essv16313364	line1 insertion	SAMN00006430	Sequencing	Read depth and paired-end mapping	Heterozygous	2,724
essv16313365	line1 insertion	SAMN00009210	Sequencing	Read depth and paired-end mapping	Heterozygous	2,753
essv16313366	line1 insertion	SAMN01091107	Sequencing	Read depth and paired-end mapping	Heterozygous	2,744
essv16313367	line1 insertion	SAMN00009253	Sequencing	Read depth and paired-end mapping	Heterozygous	2,651
essv16313368	line1 insertion	SAMN01091076	Sequencing	Read depth and paired-end mapping	Heterozygous	2,798
essv16313369	line1 insertion	SAMN00014347	Sequencing	Read depth and paired-end mapping	Heterozygous	2,721
essv16313370	line1 insertion	SAMN00014348	Sequencing	Read depth and paired-end mapping	Heterozygous	2,637
essv16313371	line1 insertion	SAMN00014351	Sequencing	Read depth and paired-end mapping	Heterozygous	2,627
essv16313372	line1 insertion	SAMN00014360	Sequencing	Read depth and paired-end mapping	Heterozygous	2,640
essv16313373	line1 insertion	SAMN00014389	Sequencing	Read depth and paired-end mapping	Heterozygous	2,670
essv16313374	line1 insertion	SAMN00014406	Sequencing	Read depth and paired-end mapping	Heterozygous	2,581
essv16313375	line1 insertion	SAMN00014420	Sequencing	Read depth and paired-end mapping	Heterozygous	2,506
essv16313376	line1 insertion	SAMN00014428	Sequencing	Read depth and paired-end mapping	Heterozygous	2,660
essv16313377	line1 insertion	SAMN00016860	Sequencing	Read depth and paired-end mapping	Heterozygous	2,865
essv16313378	line1 insertion	SAMN00249720	Sequencing	Read depth and paired-end mapping	Heterozygous	2,466
essv16313379	line1 insertion	SAMN00630200	Sequencing	Read depth and paired-end mapping	Heterozygous	3,059
essv16313380	line1 insertion	SAMN00255143	Sequencing	Read depth and paired-end mapping	Heterozygous	2,624
essv16313381	line1 insertion	SAMN00263026	Sequencing	Read depth and paired-end mapping	Heterozygous	2,671
essv16313382	line1 insertion	SAMN00262987	Sequencing	Read depth and paired-end mapping	Heterozygous	3,325
essv16313383	line1 insertion	SAMN00780005	Sequencing	Read depth and paired-end mapping	Heterozygous	2,744
essv16313384	line1 insertion	SAMN00001515	Sequencing	Read depth and paired-end mapping	Heterozygous	2,638
essv16313385	line1 insertion	SAMN00216588	Sequencing	Read depth and paired-end mapping	Heterozygous	2,759
essv16313386	line1 insertion	SAMN00001538	Sequencing	Read depth and paired-end mapping	Heterozygous	2,519
essv16313387	line1 insertion	SAMN00801704	Sequencing	Read depth and paired-end mapping	Heterozygous	2,836
essv16313388	line1 insertion	SAMN00801770	Sequencing	Read depth and paired-end mapping	Heterozygous	2,626
essv16313389	line1 insertion	SAMN00007707	Sequencing	Read depth and paired-end mapping	Heterozygous	2,707
essv16313390	line1 insertion	SAMN00007752	Sequencing	Read depth and paired-end mapping	Heterozygous	2,540
essv16313391	line1 insertion	SAMN00004477	Sequencing	Read depth and paired-end mapping	Heterozygous	2,783
essv16313392	line1 insertion	SAMN00001229	Sequencing	Read depth and paired-end mapping	Homozygous	2,893
essv16313393	line1 insertion	SAMN00001298	Sequencing	Read depth and paired-end mapping	Heterozygous	2,894
essv16313394	line1 insertion	SAMN00001320	Sequencing	Read depth and paired-end mapping	Heterozygous	2,903
essv16313395	line1 insertion	SAMN00001327	Sequencing	Read depth and paired-end mapping	Heterozygous	2,803
essv16313396	line1 insertion	SAMN00007893	Sequencing	Read depth and paired-end mapping	Heterozygous	2,867
essv16313397	line1 insertion	SAMN00007896	Sequencing	Read depth and paired-end mapping	Heterozygous	2,874

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16313355	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313356	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313357	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313358	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313359	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313360	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313361	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313362	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313363	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313364	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313365	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313366	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313367	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313368	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313369	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313370	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313371	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313372	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313373	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313374	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313375	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313376	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313377	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313378	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313379	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313380	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313381	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313382	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313383	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313384	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313385	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313386	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313387	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313388	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313389	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313390	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313391	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313392	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313393	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313394	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313395	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313396	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313397	Remapped	Perfect	NC_000021.9:g.3236 1536_32361537ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	32,361,536	32,361,536
essv16313355	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313356	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313357	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313358	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313359	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313360	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313361	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313362	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313363	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313364	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313365	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313366	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313367	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313368	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313369	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313370	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313371	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313372	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313373	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313374	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313375	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313376	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313377	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313378	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313379	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313380	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313381	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313382	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313383	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313384	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313385	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313386	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313387	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313388	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313389	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313390	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313391	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313392	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313393	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313394	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313395	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313396	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845
essv16313397	Submitted genomic		NC_000021.8:g.3373 3845_33733846ins?	GRCh37 (hg19)		NC_000021.8	Chr21	33,733,845	33,733,845

dbVar

Database of genomic structural variation

esv3646881

Links to Other Resources

Genome View

Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.